Dual‐Mode Thio‐MacMillan Organocatalysts: Stereoselective Diels–Alder Reactions or Sacrificial Self‐Cyclization to <i>N</i> ‐Bridged Bicyclic Lactams

Marian S. R. Ebeling, Luca V. Parziale, Marc Sachsenhauser, Christoph J. B. Seifert, Nathalie J. Kurrle, Oliver Trapp

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DOI: 10.1002/chem.202503017
Published: 2025-12-18
Container: Chemistry – A European Journal
Publisher: Wiley
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1002/chem.202503017,
  title = {Dual‐Mode Thio‐MacMillan Organocatalysts: Stereoselective Diels–Alder Reactions or Sacrificial Self‐Cyclization to
                    <i>N</i>
                    ‐Bridged Bicyclic Lactams},
  author = {Marian S. R. Ebeling and Luca V. Parziale and Marc Sachsenhauser and Christoph J. B. Seifert and Nathalie J. Kurrle and Oliver Trapp},
  year = {2025},
  journal = {Chemistry – A European Journal},
  doi = {10.1002/chem.202503017},
  url = {https://doi.org/10.1002/chem.202503017}
}

RIS

TY  - JOUR
TI  - Dual‐Mode Thio‐MacMillan Organocatalysts: Stereoselective Diels–Alder Reactions or Sacrificial Self‐Cyclization to
                    <i>N</i>
                    ‐Bridged Bicyclic Lactams
AU  - Marian S. R. Ebeling
AU  - Luca V. Parziale
AU  - Marc Sachsenhauser
AU  - Christoph J. B. Seifert
AU  - Nathalie J. Kurrle
AU  - Oliver Trapp
PY  - 2025
JO  - Chemistry – A European Journal
DO  - 10.1002/chem.202503017
UR  - https://doi.org/10.1002/chem.202503017
ER  -

APA

Ebeling, M. S. R., Parziale, L. V., Sachsenhauser, M., Seifert, C. J. B., Kurrle, N. J., & Trapp, O. (2025). Dual‐Mode Thio‐MacMillan Organocatalysts: Stereoselective Diels–Alder Reactions or Sacrificial Self‐Cyclization to <i>N</i> ‐Bridged Bicyclic Lactams. Chemistry – A European Journal. https://doi.org/10.1002/chem.202503017

Source records

crossref · retrieved 2026-09-26T11:27:52.515Z